chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	73968642	73968643	C	T	21	GENIC	homozygous	110778915
18	73969084	73969085	T	C	47	GENIC	homozygous	110778917
18	73969248	73969249	T	C	30	GENIC	homozygous	110778919
18	73969353	73969354	C	T	22	GENIC	homozygous	110778921
18	73969428	73969429	A	G	22	GENIC	homozygous	110556376
18	73969490	73969491	G	A	28	GENIC	homozygous	110778923
18	73969629	73969630	A	G	26	GENIC	homozygous	110778925
18	73969933	73969934	C	T	34	GENIC	homozygous	110778927
18	73969964	73969965	A	C	32	GENIC	homozygous	110778929
18	73970071	73970072	A	G	32	GENIC	homozygous	110778931
18	73970193	73970194	G	T	34	GENIC	homozygous	110778933
18	73970205	73970206	G	A	33	GENIC	homozygous	110778935
18	73970268	73970269	G	A	30	GENIC	homozygous	110778936
18	73971337	73971338	A	G	29	GENIC	homozygous	110778938
18	73971869	73971870	T	G	2	GENIC	homozygous	110778940
18	73972106	73972107	T	C	24	GENIC	homozygous	110556378
18	73972140	73972141	C	T	26	GENIC	homozygous	110778942
18	73972291	73972292	C	T	33	GENIC	homozygous	110556380
18	73972406	73972407	T	C	31	GENIC	homozygous	110556382
18	73972701	73972702	T	C	16	GENIC	homozygous	110635593
18	73972846	73972847	T	C	18	GENIC	homozygous	110556384
18	73972993	73972994	C	T	18	GENIC	homozygous	110778945
18	73973988	73973989	A	G	20	GENIC	homozygous	110778947
18	73974415	73974416	G	A	22	GENIC	homozygous	110556390